http://identifiers.org/hco/1/GRCh38#214281104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189654597-C-A

214281104-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: non coding transcript exon variant
orthologous variants: 189654597-C-G

214281104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: non coding transcript exon variant
orthologous variants: 189654597-C-T

http://identifiers.org/hco/1/GRCh38#214281111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#189654590-C-A

214281111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 189654590-C-T

http://identifiers.org/hco/1/GRCh38#214281140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189654551-C-A

214281140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: non coding transcript exon variant
orthologous variants: 189654551-C-T

214281523-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189654291-T-A

214281523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189654291-T-C

214281523-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189654291-T-G

214281620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 189654254-G-T

214282306-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189653786-G-C

214283184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189652950-C-T

214283197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189652937-C-T

214283278-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189652873-G-C

214283302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189652865-T-C

214283535-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189652680-A-T

214283754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189652509-G-T

214283846-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189652425-G-C

http://identifiers.org/hco/1/GRCh38#214283852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189652419-C-A

214283872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189652401-A-G

214287622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189650861-C-T

214287626-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189650857-T-A

214287676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189650812-G-A

214287767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189650733-T-C

214287826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189650674-T-C

214288762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189649854-T-C

214288938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189649730-C-T

214289183-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189649517-G-C

214289278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189649449-G-A

214289790-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189649061-T-A

214289917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189648963-T-C

214290382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189648493-G-A

214290911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189647899-G-T

214290935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189647876-C-T

214295720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189646804-T-C

214295793-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189646729-C-G

214295793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189646729-C-T

214296118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189646421-T-C

214296221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189646320-A-G

214296250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189646291-C-T

214296327-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189646224-T-A

214296353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189646199-A-G

214296740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189645830-A-G

214297544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189644732-T-C

214297594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189644678-G-A

http://identifiers.org/hco/1/GRCh38#214297606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189644666-C-A

214303141-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189643533-C-G

http://identifiers.org/hco/1/GRCh38#214303234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189643448-C-A

214303234-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189643448-C-G

214303234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189643448-C-T

214303435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189643274-C-T

214303801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189642949-G-A

214305041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189642224-G-T

214305061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189642209-G-A

214305061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189642209-G-T

214305076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189642195-G-A

214305090-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189642182-T-A

214305116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189642163-G-A

214305116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189642163-G-T

214305144-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189642153-T-G

214305224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189642072-G-A

214305224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189642072-G-T

214305261-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189642034-G-C

214305338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189641944-A-G

214305369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189641919-G-A

214305369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189641919-G-T

214305858-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189641499-T-G

214305859-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189641498-A-T

214305961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189641400-C-T

214306236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189640649-C-T

214306252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189640633-T-C

214306284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189640621-C-T

214306432-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189640491-G-C

214306468-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189640457-C-G

214306471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189640454-T-C

214306952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189640191-C-T

http://identifiers.org/hco/1/GRCh38#214307611-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189639768-A-C

214307682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189639718-G-A

214307696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189639704-G-A

214307980-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189639484-A-T

214308014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189639452-A-G

214308206-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189639300-T-G

214308265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189639241-C-T

214308294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189639125-A-G

214311177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189635850-T-C

214311514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189635524-C-T

214311638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189635412-A-G

214311935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189635031-G-A

214311978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189634978-T-C

214311981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189634975-C-T

214311983-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189634973-C-G

214312293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189634666-G-T

http://identifiers.org/hco/1/GRCh38#214313180-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189633872-A-C

214313269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189633787-A-G

214313290-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189633767-T-A

214313477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189633504-C-T

214314742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189632144-G-A

214314742-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189632144-G-C

http://identifiers.org/hco/1/GRCh38#214314985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189631903-C-A

214315004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189631884-A-G

214315057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189631840-T-C

214315332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189631564-T-C

214315381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189631520-G-A

214316833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189630853-G-A

214316855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189630831-T-C

214316880-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189630811-T-A

214316949-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189630742-T-G

214317068-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189630647-T-G

214317392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189630365-A-G

214317392-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189630365-A-T

214317492-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189630258-T-G

214317954-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189629792-T-G

214317995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189629756-T-C

214318021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189629730-T-C

http://identifiers.org/hco/1/GRCh38#214318158-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189629600-A-C

214318163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189629595-C-T

214318164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189629594-G-A

214318164-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189629594-G-C

214318164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189629594-G-T

214318489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189629193-G-A

214318538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189629141-G-A

214318707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189629040-G-A

214318707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189629040-G-T

214318766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189629004-G-A

214318766-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189629004-G-C

214318766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189629004-G-T

214318768-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189629002-T-A

214318768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189629002-T-C

214318768-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189629002-T-G

214318786-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189628984-T-A

214318788-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189628982-A-T

214318797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189628946-A-G

214318963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 189628786-C-T

214321527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189626846-A-G

214321556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189626818-G-A

214321568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189626806-G-A

214321683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189626726-T-C

214321746-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189626663-A-T

214321766-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189626643-T-A

214322018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189626388-G-A

214322018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189626388-G-T

http://identifiers.org/hco/1/GRCh38#214322279-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189626124-A-C

214322304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189626099-A-G

214322693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189625227-G-T

214322774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189625157-T-C

214322781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189625149-T-C

214322954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189625051-G-A

214322954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189625051-G-T

214322965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189625045-G-A

214322976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189625034-T-C

214322991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189625019-G-T

214323264-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189624809-T-G

214323557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189624476-G-A

http://identifiers.org/hco/1/GRCh38#214323572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189624471-C-A

214323803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189624300-A-G

214324783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189623522-T-C

http://identifiers.org/hco/1/GRCh38#214324869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189623436-C-A

214324961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189623349-C-T

214325024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189623294-G-T

214325092-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189623229-G-C

214325158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189623165-C-T

214325176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189623147-T-C

214325192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189623131-C-T

214326464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 189622417-A-G

214326605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 189622278-T-C

214326799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189622062-A-G

214327138-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189621763-C-G

214327138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189621763-C-T

214327331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189621594-G-A

214327355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189621570-G-T

214327375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189621448-T-C

214327394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189621429-G-T

214327416-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189621382-T-A

214327420-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189621378-T-A

214327434-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189621306-T-A

http://identifiers.org/hco/1/GRCh38#214327462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189621277-C-A

http://identifiers.org/hco/1/GRCh38#214327463-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189621276-A-C

214327463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189621276-A-G

214327463-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189621276-A-T

http://identifiers.org/hco/1/GRCh38#214327503-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189621232-A-C

http://identifiers.org/hco/1/GRCh38#214327582-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189621153-A-C

214327582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189621153-A-G

214328092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189620669-T-C

214328166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189620623-C-T

214328452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189620277-G-A

214328512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189620269-G-A

214328512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189620269-G-T

214328692-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189620157-T-G

214328805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189620069-T-C

214329073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 189619851-T-C

214329185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189619740-C-T

214329187-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189619738-T-G

214329525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189619282-A-G

214329546-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189619263-T-G

http://identifiers.org/hco/1/GRCh38#214329547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189619262-C-A

214329741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189619108-G-A

214329741-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189619108-G-C

214329992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189618939-A-G

214329996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189618935-C-T

http://identifiers.org/hco/1/GRCh38#214330321-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189618679-C-A

214330321-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189618679-C-G

214330347-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189618660-G-T

214330370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189618642-A-G

214330373-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189618639-A-T

214330374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189618638-T-C

214330378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189618630-T-C

http://identifiers.org/hco/1/GRCh38#214330391-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189618617-A-C

214330391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189618617-A-G

http://identifiers.org/hco/1/GRCh38#214330393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189618610-C-A

214330393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189618610-C-T

http://identifiers.org/hco/1/GRCh38#214330410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189618593-C-A

214330410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189618593-C-T

214330415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189618588-G-A

214330417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189618586-G-A

214330417-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189618586-G-C

214330422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189618581-T-C

214330438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189618563-C-T

214330544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189617943-A-G

214330547-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189617939-G-C

214330725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189617788-G-T

214330805-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189617705-T-A

214330805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189617705-T-C

http://identifiers.org/hco/1/GRCh38#214330808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189617702-C-A

214330808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189617702-C-T

214330870-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189617682-T-A

214330886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189617666-G-A

214330910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189617652-A-G

214331230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189617341-T-C

214331230-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189617341-T-G

214331251-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189617320-G-C

214331251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189617320-G-T

http://identifiers.org/hco/1/GRCh38#214331393-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189617201-A-C

214331409-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189617184-C-G

214331409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189617184-C-T

214331452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189617149-G-T

214331477-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189617124-T-A

214331483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189617120-A-G

214331484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189617119-T-C

214331485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189617118-T-C

214331496-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189617107-A-T

http://identifiers.org/hco/1/GRCh38#214331547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189617067-C-A

214331577-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189617044-T-G

214331606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189617032-G-T

214331709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189616507-G-T

214331719-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189616497-T-G

214331762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189616454-A-G

214331922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189616329-G-A

214331922-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189616329-G-T

214331929-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189616320-T-A

214331929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189616320-T-C

http://identifiers.org/hco/1/GRCh38#214332029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#189616182-C-A

214332199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 189616012-G-A

214332199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 189616012-G-T

214332228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189616005-G-A

http://identifiers.org/hco/1/GRCh38#214332347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189615950-C-A

214332347-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189615950-C-G

214332347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189615950-C-T

http://identifiers.org/hco/1/GRCh38#214332351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189615946-C-A

214332351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189615946-C-T

214332390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189615911-G-A

214332390-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189615911-G-C

214332390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189615911-G-T

214332432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189615889-G-A

214332432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189615889-G-T

http://identifiers.org/hco/1/GRCh38#214332488-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189615842-A-C

http://identifiers.org/hco/1/GRCh38#214332502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189615828-C-A

214332554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189615766-G-T

214332591-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189615716-T-A

214332591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189615716-T-C

http://identifiers.org/hco/1/GRCh38#214332598-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189615709-A-C

214332598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189615709-A-G

214332641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189615667-G-T

http://identifiers.org/hco/1/GRCh38#214332805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189615540-C-A

http://identifiers.org/hco/1/GRCh38#214333091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189615327-C-A

214333236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189615218-G-T

214333264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189615206-G-T

214333319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189615150-G-T

http://identifiers.org/hco/1/GRCh38#214333452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189615067-C-A

214333455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189615064-G-T

http://identifiers.org/hco/1/GRCh38#214333505-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189615015-A-C

214333505-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189615015-A-T

http://identifiers.org/hco/1/GRCh38#214333540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189614978-C-A

214333594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189614924-A-G

http://identifiers.org/hco/1/GRCh38#214333639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189614878-C-A

214333645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189614872-G-A

214333645-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189614872-G-T

214333681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189614829-G-T

214333766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189614768-G-A

214333768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189614766-G-T

214333829-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189614703-C-G

http://identifiers.org/hco/1/GRCh38#214333872-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189614664-A-C

214333872-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189614664-A-T

214333889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189614647-A-G

214333889-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189614647-A-T

214333937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189614600-A-G

214333937-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189614600-A-T

http://identifiers.org/hco/1/GRCh38#214333959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189614578-C-A

214333976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189614561-G-T

214334032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189614507-G-A

214334032-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189614507-G-T

http://identifiers.org/hco/1/GRCh38#214334051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189614490-C-A

214334051-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189614490-C-G

214334051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189614490-C-T

http://identifiers.org/hco/1/GRCh38#214334063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189614478-C-A

214334063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189614478-C-T

214334066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189614475-G-T

214334270-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 189614342-C-G

214334270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 189614342-C-T

http://identifiers.org/hco/1/GRCh38#214334419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189614194-C-A

214334419-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189614194-C-G

214334419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189614194-C-T

214334687-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189614003-G-T

214336731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 189613034-G-A

http://identifiers.org/hco/1/GRCh38#214336740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189613025-C-A

214336843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 189612938-G-T

214336973-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 189612849-T-A

214337059-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 189612761-T-A

214337059-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20982
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 189612761-T-G